|Publication number||US4113645 A|
|Application number||US 05/819,517|
|Publication date||12 Sep 1978|
|Filing date||26 Jul 1977|
|Priority date||26 Jul 1977|
|Also published as||CA1086006A, CA1086006A1, DE2832135A1|
|Publication number||05819517, 819517, US 4113645 A, US 4113645A, US-A-4113645, US4113645 A, US4113645A|
|Inventors||Robert Santora DeSimone|
|Original Assignee||Polak's Frutal Works, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (4), Referenced by (61), Classifications (16)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This invention relates to the preparation of bleach solutions containing perfume oils to mask the unpleasant chlorine odor which is characteristic of such solutions.
The problem associated with the perfuming of an alkali metal hypochlorite bleach solution is a two-part problem. First, such bleach solutions are aqueous systems, and since most fragrance compositions are not soluble in aqueous systems, an appropriate surfactant must be found for dispersing the perfume in the bleach to form a stable emulsion. The surfactant must be one which is unaffected or substantially unaffected by the strong oxidizing and alkali action of the bleach. Second, perfume oils or perfume compositions must be used which likewise are impervious to the oxidizing action of the bleach.
If either the surfactant or the perfume is unstable in the presence of the alkali metal hypochlorite, the effect of the perfume will be lost. A more serious problem, however, is that the alkali metal hypochlorite will be consumed by reaction with the additive and thus the strength of the solution will be lowered, rendering it less effective for its intended use as a household bleach or disinfectant.
The concept of a perfumed bleach composition has been advanced previously. For example, U.S. Pat. No. 3,684,722 teaches that an alkali hypochlorite bleach solution thickened with a mixture of an alkali metal soap and an amine oxide or a long chain substituted betaine can be perfumed, but that the addition of perfume leads to a reduction in stability of the thickened solution. U.S. Pat. No. 3,876,551 teaches preparation of similar compositions based on amine oxides but without the alkali metal soap. Omission of the soap is said to be desirable in order that perfume oils having "clean fresh", "floral", "woody", "musk" or "citrusy" odors can function properly.
Neither of the cited references, however, appears to provide a solution to the problem of long term stability. There is no suggestion that the bleach is substantially undiminished in strength or that the fragrance characteristics of the perfume oils are unaltered upon long term storage. It is an object of this invention to provide perfumed hypochlorite bleach compositions which are stable over relatively long periods of time.
It is a further object of this invention to provide stable perfumed bleach compositions having a variety of odor types.
It is yet another object of this invention to provide surfactants capable of dispersing a perfume oil in a hypochlorite bleach solution, which surfactants are inert to the oxidizing action of the bleach over long periods of storage time.
These and other objects of the invention are accomplished by dispersing a perfume oil in an aqueous solution of an alkali metal hypochlorite using, as a dispersant, a quaternary ammonium compound of the general formula ##STR1## where R1 is an alkyl or aromatic group containing from about 1 to 20 carbon atoms, R2 through R7 are selected from the group consisting of alkyl and aromatic groups containing about 1 to 14 carbon atoms, cycloalkyl groups containing about 5 to 18 carbon atoms, alkaryl groups containing from 7 to 10 carbon atoms, and pyridyl groups, and X is selected from the group consisting of fluoride, chloride, nitrate, sulfate, methyl sulfate, carbonate, sulfonate, chlorate and hydroxide and n is either 1 or 2 and is equal to the valence of X.
Typical quaternary ammonium salts useful in the bleach compositions of this invention are hexadecyl trimethyl ammonium chloride, dodecyl trimethyl ammonium chloride, pentadecyl triethyl ammonium chloride, dimethyl stearyl benzyl ammonium chloride, tetradecyl trimethyl ammonium chloride, hexadecyl trimethyl ammonium chloride, and mixtures of these materials. Two preferred quaternary compounds are hexadecyl trimethyl ammonium chloride and dodecyl trimethyl ammonium chloride.
It will be apparent that the perfume oils suitable for use in this invention are those materials which are resistant to the oxidative effects of the bleach or to the alkali action of the alkali metal hypochlorite solution. As employed herein, the term "perfume" or "perfume oil" is intended to include both individual, unblended compounds and blended compositions comprised of a number of specific, identifiable chemical compounds. The preferred classes of fragrance ingredients meeting these requirements are such materials as aromatic heterocyclic nitrogen compounds such as quinolines, pyridines and pyrazines, aliphatic or aromatic acetals, aliphatic or aromatic ethers, aliphatic or aromatic nitriles, tertiary alcohols, and cyclic oxides. Obviously, not every compound within these classes is a useful perfume oil, but any which are otherwise useful and which do not contain substituent groups which are sensitive to alkali metal hypochlorite or to alkali are useful. Substituent groups which are sensitive and which cannot be present are such groups as active methylene groups adjacent to an aromatic ring, esters, C-C double bonds, ketones or aldehydes with enolizable hydrogens, primary or secondary alcohols, and free phenolic hydroxyls.
Among specific perfume oils found stable upon long term storage in contact with liquid alkali metal hypochlorite solutions are 1,8-cineole, 2-isobutyl quinoline, 2-hexyl pyridine, dihydro-8-terpineol, tetrahydrolinalool, paracresyl methyl ether, heptanal diethyl acetal, beta-naphthyl ethyl ether, diphenyl oxide, cedrol, diphenyl ketone, dihydroanethole, acetaldehyde ethyl-betaphenyl ethyl acetal, resorcinol dimethyl ether, diphenyl oxide, tertiary amyl cymene, dimethyl phenyl carbinol, 2-ethyl-3,5-dimethyl pyrazine, 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethyl cyclopenta-gamma-2-benzopyran and methyl phenyl ethyl ether.
A typical alkali metal hypochlorite solution employed as a household bleach contains about 5% of sodium hypochlorite. Solutions varying from about 1 to 15% hypochlorite can be used, however. Any of the alkali metal hypochlorites can be used; sodium hypochlorite is preferred.
The amount of quaternary ammonium salt required to disperse the perfume oil in the aqueous bleach solution is between about 0.025 and 1% based on the weight of alkali metal hypochlorite solution. While the precise amount in any instance varies, depending upon the amount and type of perfume oil used and the type of dispersion desired, as a rule of thumb, it is usually found that the amount of dispersant employed is no greater than about three times the weight of perfume oil employed.
The amount of perfume oil added to the bleach solution depends upon the type of oil used and the strength or odor effect desired. Since most perfume oils are relatively expensive as compared to the market price of the bleach solution, the upper limit of perfume oil for economic reasons can usually not exceed about 0.5% based on the weight of the bleach solution. Normally, the amount is between about 0.02 and 0.3% and preferably between about 0.05 and 0.15%.
The following examples illustrate the invention but are not intended to be limiting. Parts and percentages are by weight unless otherwise specified.
A perfume was compounded in the following proportions:
______________________________________ Parts______________________________________Diphenyl oxide 140Cedryl methyl ether 10Tetrahydrolinalool 100Acetaldehyde ethyl, beta-phenyl ethyl acetal 301,8-Cineole 200Tetrahydromuguol (IFF Register) 50Acetaldehyde methyl ethyl acetal 101,1-Diethoxy heptane 10Isobutanal diethyl acetal 220Phenyl acetaldehyde dimethyl acetal 10Hydrotropic aldehyde dimethyl acetal 102-Isobutyl quinoline 5Dihydroterpinyl acetate 10Resorcinol dimethyl acetal 5______________________________________
This perfume was added with shaking at 0.1% concentration to commercial 5.1% sodium hypochlorite bleach solution containing 0.3% of a 29% aqueous solution of hexadecyl trimethyl ammonium chloride (Arquad 16-29 -Armak Industrial Chemicals Division of Akzona, Inc.). After 14 months of storage at room temperature shielded from light, the mixture still possessed a strong odor of the original perfume quality. A sample of the original unperfumed bleach showed 3.7% hypochlorite (72.5% of original) after the 14-month storage period, while the perfumed bleach sample showed 2.7% sodium hypochlorite (53% of original).
Three perfumes containing various proportions of:
Beta-naphthyl ethyl ether
Paracresyl methyl ether
Acetaldehyde ethyl - beta-phenyl ethyl acetal were added, with shaking, separately at 0.05% concentration to three separate portions of liquid bleach, which contained 0.05% hexadecyl trimethyl ammonium chloride and placed in an oven at 55° C. After 72 hours in the oven at 55° C., all samples still retained some fragrance.
The following materials were combined (3 drops) with 50 ml. of commercial 5.1% sodium hypochlorite solution and 9 drops of 29% hexadecyl trimethyl ammonium chloride solution were added, with shaking, to give a dispersion. Periodic observations were made, as shown below, after the solution was allowed to stand at ambient temperature shielded from light:
______________________________________Compound CommentsFragrance from Example 2 24 days, odor still strong 3 months, odor still presentDihydroanethole 3 months, odor still strongResorcinol dimethyl ether 3 months, odor still presentPhenyl acetaldehyde 3 months, odor still presentdimethyl acetateIsobutyl quinoline 3 months, odor strong1,1-Diethoxyheptane 3 months, some odor still presentIsobutanal diethyl acetal 3 weeks, odor strong 3 months, little odorDihydroterpinyl acetate 3 weeks, odor still strong 3 months, odor somewhat diminished______________________________________
Three fragrances were made up of the following ingredients:
______________________________________ Fragrance #1 #2 #3______________________________________Eucalyptus oil (1,8-cineole) 800 900 930Cedryl methyl ether 50 60 50Dihydroanethole 10 40 19Tetrahydrolinalool 140 0 0Tetrabutyl quinoline 0 0 1Total parts 1000 1000 1000______________________________________
Each fragrance was added to commercial 5.1% sodium hypochlorite liquid bleach at 0.1% concentration in three separate 50-ml. portions, which contained 0.05%, 0.3%, and 0.15%, respectively, of 29% hexadecyl trimethyl ammonium chloride solution. All solutions were virtually clear upon mixing of the ingredients. Periodic observations were made on the samples as shown below.
__________________________________________________________________________ % Observations Surfactant 2 Weeks 2 Months 3 Months 6-1/2 Months__________________________________________________________________________Fragrance I 0.05 Slightly hazy, Slightly hazy, Slightly hazy, Clear, odor good, odor strong odor strong odor strong slight ppt. on bottom 0.15 Slightly hazy, Slightly hazy, Slightly hazy, Clear, odor good, odor strong odor strong odor strong slightly hazy 0.30 Slightly hazy, Slightly hazy, Slightly hazy, Clear, odor strong odor strong odor strong odor strongFragrance II 0.05 Clear, odor Clear, odor strong strong Clear, odor Clear, odor good, strong slight ppt. on bottom 0.15 Clear, odor Clear, odor Clear, odor Clear, odor good, strong strong strong slightly hazy 0.30 Clear, odor Clear, odor Clear, odor Clear, odor strong strong strong strongFragrance III 0.05 Clear, odor Clear, odor Clear, odor Clear, odor strong, strong strong strong slight ppt. on bottom 0.15 Clear, odor Clear, odor Clear, odor Clear, odor strong, strong strong strong slightly hazy 0.30 Clear, odor Clear, odor Clear, odor Clear, odor strong strong strong strong__________________________________________________________________________
A fragrance formulated as shown below:
______________________________________1,8-Cineole 930 partsCedryl methyl ether 50 partsDihydroanethole 19 parts2-Isobutyl quinoline 1 part______________________________________
was added at 0.05% to 5.0% aqueous sodium hypochlorite solution containing 0.2% hexadecyl trimethyl ammonium chloride and the mixture was stirred until homogeneous. After 61/2 months' storage at ambient temperature, shielded from light, the mixture was found somewhat turbid, while the fragrance was strong.
A fragrance, formulated as in Example 5, was added at 0.2% to two portions of 5.1% commercial sodium hypochlorite solution, containing 0.2% and 0.4%, respectively, of hexadecyl trimethyl ammonium chloride. The solution containing 0.2% quaternary was slightly turbid initially, after mixing, while the one containing 0.4% was clear. After three months, at ambient storage conditions, the solution containing 0.2% quaternary was hazy with a strong odor of perfume still present, while the 0.4% solution was opaque, but still possessing a strong fragrance aroma.
A mixture of 0.05% fragrance, formulated as in Example 5, and 0.2% hexadecyl trimethyl ammonium chloride in 5.1% sodium hypochlorite solution was found clear after initial mixing. After six weeks, some gelatinous precipitate was present, with the perfume odor quite strong. After four months of storage, under ambient conditions, shielded from light, the solution was turbid, the odor satisfactory.
(a) A solution of 3 drops of diphenyl methane and 9 drops of a 30% aqueous solution of hexadecyl trimethyl ammonium chloride in 25 ml. of 5.1% sodium hypochlorite was shaken, to aid dispersion, and stored for 4 months at ambient temperature, at which point the odor of the diphenyl methane was absent.
(b) A solution of 3 drops of a mixture of 2,6-dimethyl-2-octanol and tetrahydrolinalool (mixture known commercially as Tetrahydromuguol, IFF Register) and 9 drops of a 20% aqueous solution of hexadecyl trimethyl ammonium chloride was stored, at ambient temperature, for 4 months, whereupon the odor of the fragrance material was still strong and the hypochlorite strength of the solution tested out at 4.35% hypochlorite. The original 5.1% hypochlorite solution, after the same four-month period, tested at 4.85% hypochlorite.
In a similar manner, the following fragrance materials were storage-tested with results as tabulated below.
__________________________________________________________________________ % HypochloriteMaterial Storage Period Odor Remaining__________________________________________________________________________1,4-Cineole 4 months Nil --1,8-Cineole 4 months Strong --Acetaldehyde ethyl methyl acetal 4 months Strong --Beta-phenyl ethyl methyl ether 4 months Strong --Cedryl methyl ether 4 months Strong 4.05% 6 months Strong --Diphenyl oxide 4 months Strong --Perfume from Example 1 3 months Strong 4.55%Perfume from Example 1 4 months Strong 4.10%2-Isobutyl Quinoline 4 months Strong 4.05%Dihydroanethole 4 months Strong 4.35%Ortho-methoxybenzyl ether 4 months Strong --1,1-Diethoxy heptane 4 months Moderate --__________________________________________________________________________
A fragrance formulated as in Example 5 was added at 0.05% level to 5.0% aqueous sodium hypochlorite solution containing 0.2% hexadecyl trimethyl ammonium chloride (Variquat E228 - Ashland Chemical Company) and the mixture stirred until homogeneous. After 61/2 months' storage at ambient temperature, shielded from light, the mixture was found somewhat turbid, but the fragrance persisted in strength.
A fragrance formulated as in Example 5 was added at 0.05% level to 5.0% aqueous sodium hypochlorite solution containing 0.6% of a mixture of 5% octyl, 6% decyl, 51% dodecyl, 19% tetradecyl, 9% hexadecyl and 5% octadecyl trimethyl ammonium chlorides (Arquad C-33 - Armak Industrial Chemicals Division of Akzona, Inc.) and the mixture stirred until homogeneous. After 61/2 months of storage at ambient temperature, shielded from light, the perfume in the mixture had retained its odor potency.
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|U.S. Classification||252/186.44, 512/2, 8/108.1, 252/187.26|
|International Classification||C11D3/395, C11D1/62, D06L3/06, C11D3/50|
|Cooperative Classification||C11D3/3956, C11D3/50, C11D1/62, D06L4/23|
|European Classification||C11D1/62, C11D3/50, C11D3/395H, D06L3/06L|